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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9145Erstellt: 23. Oktober 2026

Boric Acid → 1-(6-(3-Aminophenyl)-2-benzothiazolyl)-3-ethylurea

https://huagongshe.com/de/reaction/9145

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoric AcidHCID 7628—
EduktSodium BicarbonateHCID 516892—
Edukt3-Aminophenylboric acidHCID 21895836—
Edukt1-(6-Bromo-2-benzothiazolyl)-3-ethylureaHCID 21985564—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelMethanolHCID 887—
LösungsmittelN,N-Dimethylformamide--water (1/1)HCID 21962138—
Produkt1-(6-(3-Aminophenyl)-2-benzothiazolyl)-3-ethylureaHCID 2198557523,4%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A suspension of 1-(6-bromo-2-benzothiazolyl)-3-ethylurea (0.300 g, 1.00 mmol), 3-aminophenyl boric acid (0.237 g, 1.50 mmol, 1.5 eq), and sodium bicarbonate (0.210 g, 2.50 mmol, 2.5 eq) in 8 mL of mixed solvent DMF/water (5/1) was purged with nitrogen gas. To the mixture, the catalyst Pd(PPh3)4 (0.058 g, 0.05 mmol, 0.05 eq) was added. It was purged with nitrogen gas again, and was heated at about 100° C. in a sealed tube for about 48 hours. More Pd(PPh3)4 (0.025 g, 0.02 mmol, 0.02 eq) and more boric acid (0.080 g, 0.50 mmol, 0.50 eq) were added after the first 24 hours. The mixture was taken up in MeOH, concentrated, dissolved in methylene chloride, washed with sodium bicarbonate solution, dried (MgSO4), evaporated, and purified by flash chromatography on SiO2 with MeOH and methylene chloride (1/50) to give the desired compound 0.073 g (23%). LC/MS 313.2 (M+1); LC retention time 2.11 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091227B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-1d4c968dd1784c18a9903db176fc40d0
Quellennotizuspto-grants-2006_08